Evidence map›Paper›PMID 37188903›Full record

ArticlePharmacological reports : PR2023

Melatonin increases collagen content accumulation and Fibroblast Growth Factor-2 secretion in cultured human cardiac fibroblasts.

Marta Drobnik, Agnieszka Tomaszewska, Joanna Ryżko, Aleksandra Kędzia, Małgorzata Gałdyszyńska, Lucyna Piera, Justyna Rydel, Jacek Szymański, Jacek Drobnik

Open access · hybridAbstract read
In one paragraph

Article in Pharmacological reports : PR, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 4 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Marta DrobnikLaboratory of Connective Tissue Metabolism, Department of Pathophysiology, Medical University of Lodz, Zeligowskiego 7/9, 90-752, Lodz, Poland.
Agnieszka TomaszewskaLaboratory of Connective Tissue Metabolism, Department of Pathophysiology, Medical University of Lodz, Zeligowskiego 7/9, 90-752, Lodz, Poland.
Joanna RyżkoLaboratory of Connective Tissue Metabolism, Department of Pathophysiology, Medical University of Lodz, Zeligowskiego 7/9, 90-752, Lodz, Poland.
Aleksandra KędziaLaboratory of Connective Tissue Metabolism, Department of Pathophysiology, Medical University of Lodz, Zeligowskiego 7/9, 90-752, Lodz, Poland.
Małgorzata GałdyszyńskaLaboratory of Connective Tissue Metabolism, Department of Pathophysiology, Medical University of Lodz, Zeligowskiego 7/9, 90-752, Lodz, Poland.
Lucyna PieraLaboratory of Connective Tissue Metabolism, Department of Pathophysiology, Medical University of Lodz, Zeligowskiego 7/9, 90-752, Lodz, Poland.
Justyna RydelLaboratory of Connective Tissue Metabolism, Department of Pathophysiology, Medical University of Lodz, Zeligowskiego 7/9, 90-752, Lodz, Poland.
Jacek SzymańskiCentral Scientific Laboratory, Medical University of Lodz, Ul. Mazowiecka 6/8, 92-215, Lodz, Poland.
Jacek DrobnikLaboratory of Connective Tissue Metabolism, Department of Pathophysiology, Medical University of Lodz, Zeligowskiego 7/9, 90-752, Lodz, Poland. drob@op.pl.ORCID http://orcid.org/0000-0002-7329-7613
Medical University of Lodz · PL

Funding

Uniwersytet Medyczny w Lodzi 503/6-103-02/503-61-001-19-00
6 · The paper itself

Abstract

backgroundThe extracellular matrix serves as a scaffold for cardiomyocytes, allowing them to work in accord. In rats, collagen metabolism within a myocardial infarction scar is regulated by melatonin. The present study determines whether melatonin influences matrix metabolism within human cardiac fibroblast cultures and examines the underlying mechanism.

methodsThe experiments were performed on cultures of cardiac fibroblasts. The Woessner method, 1,9-dimethylmethylene blue assay, enzyme-linked immunosorbent assay and quantitative PCR were used in the study.

resultsMelatonin treatment lowered the total cell count within the culture, elevated necrotic and apoptotic cell count as well as augmented cardiac fibroblast proliferation, and increased total, intracellular, and extracellular collagen within the fibroblast culture; it also elevated type III procollagen α1 chain expression, without increasing procollagen type I mRNA production. The pineal hormone did not influence matrix metalloproteinase-2 (MMP-2) release or glycosaminoglycan accumulation by cardiac fibroblasts. Melatonin increased the release of Fibroblast Growth Factor-2 (FGF-2) by human cardiac fibroblasts, but cardiotrophin release was not influenced.

conclusionWithin human cardiac fibroblast culture, collagen metabolism is regulated by melatonin. The profibrotic effect of melatonin depends on the elevation of procollagen type III gene expression, and this could be modified by FGF-2. Two parallel processes, viz., cell elimination and proliferation, induced by melatonin, lead to excessive replacement of cardiac fibroblasts.

Indexed as

MelatoninCells, CulturedCollagenCollagen Type IFibroblast Growth Factor 2FibroblastsHumansMatrix Metalloproteinase 2CollagenCollagen Type IFibroblast Growth Factor 2Matrix Metalloproteinase 2MelatoninProcollagen Type ICell culturesCollagenConnective tissueFibroblastGlycosaminoglycanHeartMelatoninProliferation

Identifiers

PMID37188903
PMCPMC10227126
OpenAlexW4376608624

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.